AMERICAN ACADEMY OF PEDIATRICS The Use of Whole Cow`s
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AMERICAN ACADEMY OF PEDIATRICS The Use of Whole Cow`s
AMERICAN The Use ACADEMY of Whole Cow’s Committee The Committee on Nutrition continues to monitor and review nutritional issues concerning the use of whole cow’s milk (WCM) in the diets of infants. The goal of those concerned with infant nutrition is the provision of an optimal diet. The recommendations in this statement replace those provided in the 1983 statement, “The Use of Whole Cow’s Milk in Infancy.” The 1983 statement focused primarily on the issue of iron nutriture in infancy. In a broader context, the statement addressed a substantial number of often controversial nutrition issues, defined as “research needs,” surrounding the appropriateness of using whole cow’s milk for infants during the first 12 months. The purpose of this statement is to provide new recommendations on the optimal feeding of infants. The use of skim milk and reduced-fat milk (eg, 2% milk) remains inappropriate during the first year of life and will not be reviewed in this statement. REVIEW OF PREVIOUS STATEMENTS During the last 20 years, the use of whole cow’s milk in infancy has been discussed by the Committee on Nutrition principally, but not exclusively, in the context of meeting infants’ iron needs. In 1969, an extensive commentary2 reviewed iron requirements in infancy, and in 1971, a policy statement3 recommended that iron-fortified formulas be used for the first 1 2 months of life. Those recommendations were prompted by a significant prevalence of iron deficiency in older infants associated with the extensive use of whole cow’s milk in later infancy. “Fluid whole milk (available in bottle or carton) or evaporated milk, both of which contain only trace amounts of iron, are substituted at the time of greatest iron need and highest prevalence of iron deficiency anemia.”3 Several clinical studies demonstrated that feeding iron-fortified formulas to infants for the first 12 months resulted in excellent iron status.47 The Committee believed that adding iron to the infant’s major source of calories (milk-based formula) was a practical and effective method to alleviate the high prevalence of iron deficiency anemia. In 1976, the Committee on Nutrition issued a statement8 recommending the use of either iron-fortified formula or infant cereal during older infancy. The Committee noted the following; “Infant formula and other heat-treated milk products are preferable The recommendations in this statement do not indicate an exclusive of treatment or procedure to be followed, Variations, taking into individual circumstances, may be appropriate. PEDIATRICS (ISSN 0031 4005). Copyright © 1992 by the American emy of Pediatrics. OF PEDIATRICS course account Acad- on Milk in Infancy Nutrition to fresh [pasteurized] cow’s milk as substitutes for breast milk feeding during the first 6 to 1 2 months of life because excessive ingestion of fresh cow’s milk may contribute to iron deficiency by increasing gastrointestinal blood lOS5.8 In 1983, the Committee on Nutrition developed a new position,’ based largely on a study by Fomon et al9 of gastrointestinal blood loss in infants aged 4 to 6 months fed WCM, heat-treated WCM, or infant formula. All infants received supplemental ferrous sulfate and ascorbic acid. Enteric blood loss was greatest in WCM-fed infants younger than 4#{189} months of age. In infants between 4’/2 and 6 months of age, there was no difference among the three groups (WCM, heat-treated WCM, or infant formula) in the number of guaiac-positive stools, mean hemoglobin levels, serum iron levels, iron binding capacity, or transferrin saturation. Consequently, the 1983 statement’ suggested that whole cow’s milk could replace iron-fortified formulas when infants older than 6 months of age were consuming at least one third of their calories from supplemental foods. The question of whether feeding iron-fortified formula to infants for the first 6 months of life would be suffiaent to prevent iron deficiency during the next 6 months when they are started on whole cow’s milk could not be answered from the existing data. REVIEW 1983 OF RESEARCH STATEMENT2 ON MILK QUESTIONS POSED THE “USE OF WHOLE IN INFANCY.” IN THE COW’S Since the 1983 recommendations, several new studies have been published that address the five questions posed in this statement. Results of these studies require further refinement regarding the feeding recommendations for later infancy. 1. “What infant is the rate and gastrointestinal variability mucosal of maturation of barrier function?” The gastrointestinal tract is immature early in life. Consequently, there is an increased transfer of intact dietary protein from the intestinal lumen into the circulation in the immediate neonatal period, particularly in preterm infants and infants who have gut injury.dlu Although controversial, it is believed that increased intestinal permeability may contribute to the high incidence of cow’s milk protein allergy, a condition that affects 0.4% to 7.5% of the infant population.” There is no information to suggest that WCM is more allergenic than infant formulas that contain intact cow’s milk proteins. Infants with cow’s milk protein allergy should not be fed either WCM or Downloaded from by guest on October 1, 2016 PEDIATRICS Vol. 89 No. 6 June 1992 1105 formulas containing intact WCM proteins. In nonallergic infants, the introduction of whole cow’s milk should be based on digestive and nutritional considerations, not on the development of the mucosal barrier. 2. “What is the relative importance of the amount and bioavailability of iron in the total diet when whole cow’s milk is substituted for iron-enriched formula at 6 months of age? Does iron-fortified cereal meet the infant’s need for iron?” Six studies’2’7 (Second National Survey based Health Department of on four independent surveys and Nutrition Examination Agriculture Food Consump- tion, Ross Mothers Study, and Gerber Nutritional Survey) have been published to date and reviewed. Five of the six studies suggest that infants fed whole cow’s milk in later infancy have median iron intakes below the recommended daily allowance. These results clearly indicate that an insufficient quantity of iron-fortified infant cereal is currently incorporated into the diet of most infants to meet iron needs. However, infant cereal is the single largest source of iron from infant solid foods available in the United States. Parents who feed their infants whole cow’s milk must also judiciously select solid foods that contain iron. The bioavailability of electrolytic iron, the form of iron that is added to infant foods, remains incompletely defined and controversial. Furthermore, quantitative studies of electrolytic iron absorption have been conducted only with adult subjects. Electrolytic iron is produced by electrolytic deposition of iron that is mechanically commuted to powder (grade A-131). Fomon’8 notes that cereals marketed in the United States and Canada containing electrolytic iron are fortified with 45 mg of iron/100 g of dry weight, or approximately 7 mg of iron/100 g of cereal as fed (ie, after dilution with milk or formula). Forbes et al,’9 using a farina-based meal, demonstrated absorption of iron of a similar particle size to be 75% that of ferrous sulfate. Elwood2#{176} demonstrated that absorption of commercially used iron powder in baked bread is about 5% that of ferrous sulfate. Fomon,’8’2’ using Elwood’s data, calculated that absorbed iron from infant cereal could only account for 0.12 mg of the 0.6 to 0.7 mg of absorbed iron that infants require each day. Both Fomon and Elwood concluded that without evidence of adequate bioavailability, the electrolytic iron used in infant cereals is not sufficient to meet the iron needs of infants fed whole cow’s milk. The composition of whole cow’s milk (ie, high calcium, high phosphorus, and low vitamin C) may decrease the bioavailability of iron from other dietary sources such as infant cereals.22 Three studies2325 compared the iron status of infants receiving ironfortified formulas for the first 6 months of life and then fed WCM or iron-fortified formulas in accordance with the 1983 American Academy of Pediatrics recommendations for the next 6-month period. In all three studies, iron status was significantly poorer in infants fed WCM. Fortification of other infant foods, including wetpack cereal-fruit products, grape juice, or milk forti- 1106 USE OF WHOLE COW’S fied with a highly bioavailable form of iron (ferrous sulfate with vitamin C), but less modified than regular infant formula, appear promising,26 but largely unexplored in the United States. Haschke et al27 demonstrated indices of iron adequacy similar to infants fed only iron-fortified formula using meat-containing infant foods fortified with ferrous sulfate and ascorbic acid that are commercially available in Austria and the Federal Republic of Germany, but not in the United States. Stekel et al28 in Chile studied the bioavailability of ferrous sulfate-fortified (elemental iron, 10 to 19 mg/L) low-fat and whole milks (less modified than regular commercial formula) fed to infants, many of whom were iron-deficient. Iron absorption from milk containing ascorbic acid (100 mgI L) ranged from 5.9% to 1 1 .3% and was not influenced by the amount of milk fat, the addition of carbohydrate, or acidification. Results of longitudinal field trials of infants from age 3 to 1 5 months with a fullfat iron-fortified acidified milk showed effective elimination of iron deficiency.29 Evidence now suggests that the current feeding practice in the United States of using iron-fortified cereal does not meet the requirement for iron when WCM is used during the second 6 months of life. This may be due to poor compliance or insufficient bioavailability of electrolytic iron. However, providing iron-fortified formula and cereal for the first 12 months, as utilized in the Women, Infants, and Chilthen Program, has been successful in reducing iron 331 3. “Can the change to cow’s milk when the infant is 6 months old produce anemia from occult blood loss when the milk is fed in excessive amounts and there is no iron supplementation?” This question has been the subject of additional study and commentary. Both Woodruff32 and Wilson33 concluded that blood loss did occur in infants fed WCM after 6 months of age. Following the gastrointestinal blood loss study by Fomon et al,9 Ziegler et al34 used a more sensitive assay for stool hemoglobin in a second study of blood loss in 6month-old infants fed either infant formula or WCM without iron supplementation. Intestinal blood loss increased in 30% of infants fed WCM but did not increase in the formula-fed group, even though all were previously fed iron-fortified formula or were breast-fed in the first 6 months of life.34 One infant in the WCM group was removed from the study because of iron deficiency. The investigators concluded that infants fed WCM had a nutritionally significant loss of iron in the stools. These studies clearly show that blood loss will occur in a substantial percentage of infants who receive WCM for the first time after 6 months of age. On the basis of these recent results,34 Fomon and Ziegler reversed their earlier positions,9 stating that they no longer recommended WCM in the second 6 months, but preferred breast milk or iron-fortified formula for the first 12 months of life.35’36 The reasons for these recommendations include the substantial enteric blood loss in infants fed WCM, the probable low bioavailability of iron absorbed from infant cereals, and the probable Downloaded from by guest on October 1, 2016 MILK inhibition of iron concentrations concentration and WCM due phosphorous to high and low acid. relative importance of the high solute cow’s milk in the total feeding 6- to 12-month-old infant? For example, the high-solute load of whole cow’s by other foods in the diet?” that have “What is the relative importance of the nutrients present in whole cow’s milk but present in infant formula and breast milk, ie, essential fatty acids, tocopherol, ascorbic acid? How much of these nutrients are obtained from the other foods commonly used in the 6- to 12-month age group?” daily allowance’2”3 linoleic acid energy intake, 3% was for not formula below However, the reduced well below the not than median intake inof dramatically to 1 .8% of total the recommended level of infants (3.7 intake WCM-fed ± 2.6 of mg/d ainvs 10.9 ± 3.1 mg/d). Moreover, a-tocopherol status, as assessed by plasma concentrations, was significantly greater in the formula-fed infants (1 14 ± 0.42 vs 0.86 ± 0.28). The studies of the past 7 years demonstrate the difficulty of providing a balanced diet for older infants when WCM replaces breast milk or iron-fortified formula. Nutrients from commonly consumed . solid foods do not complement DEFICIENCY AND studies by Oski and co-workers38 show that deficiency in infants and children is associated subtle behavioral differences. Additional recent studies3942 suggest that iron deficiency in early childhood may lead to long-term changes in behavior that may not be reversed even with iron supplementation sufficient to correct the anemia. Newly published studies on iron deficiency and behavior show the importance of iron deficiency in WCM-fed infants. The biochemical mechanism linking iron deficiency nutrients from and behavior WCM; rather, they exaggerate the deficiencies (iron, linoleic acid, and vitamin E) and excesses (sodium, potassium, chloride, and protein) in the infant’s diet. may Youdim’s group researchers have be identified from in experimental shown mechanism in which studies that the number These of dopamine is reduced when the a transient period of and are not subsesupplementation. Aland further amplia possible model of a a transient nutritional event produce long-term changes in the neurologic of the brain of the animal studied. Additional is necessary to understand the implications deficiency to possible brain from animals.4345 D-2 receptors in the rat brain experimental animals undergo iron deficiency during infancy quently restored with iron though they require confirmation fication, these studies provide dysfunction may status research of iron in humans. SUMMARY The pediatrician is faced with a difficult challenge in providing recommendations for optimal nutrition in older infants. Because the milk (or formula) portion of the diet represents 35% to 100% of total daily calories and because WCM and breast milk or infant formula differ markedly in composition, the selection of a milk or formula has a great impact on nutrient intake. Infants fed and potassium, reduced the recommended study37 of 97 older infants, was significantly lower in in formula-fed ON IRON BEHAVIOR acid, 1’,16 In one tocopherol fants of WCM acid, but STUDIES Earlier several studies show of infant formula Substitution take of ascorbic NEW iron with infants fed a markedly increased intake of sodium, potassium, chloride, and protein.’2’6 The sodium intake (1000 mg/d) of WCMfed infants substantially exceeds the estimated minimum requirements (120 mg/d for infants from birth to 5 months old and 200 mg/day for infants 6 to 11 months old). By comparison, the median sodium intake for formula-fed infants (7 to 1 2 months old) is 580 mg/d.’2 Consequently, the renal solute load of WCM-fed infants exceeds that of formula-fed infants by twoto threefold (from approximately 1 25 to 300 mOsm).’6 Ziegler36 calculated the potential renal solute load of two hypothetical infants, 6- and 10months-old, fed infant solids and formula versus infant solids and WCM. When WCM replaced formula, the potential renal solute load increased twofold in the 6-month-old infant (42 vs 21 mOsm/100 kcal) and nearly twofold in the 10-month-old infant (39 vs 26 mOsm/100 kcal). He concluded that both infants exceeded their recommended maximum (33 mOsm/100 kcal) potential renal solute load when fed WCM and that WCM feeding would narrow the margin of safety in situations that may lead to dehydration. Thus, the high renal solute load of WCM was not diluted by other foods in the diet. 5. from instead in calcium of ascorbic 4. “What is the load of whole regimen of a how much of milk is diluted Data WCM availability of WCM vitamin and have E, and low intakes excessive protein, illustrating of iron, intakes the linoleic of sodium, poor nutri- tional compatibility of solid foods and WCM. These nutrient intakes are not optimal and may result in altered nutritional status, with the most dramatic effect on iron status. Infants fed iron-fortified formula or breast milk for the first 1 2 months of life generally maintain normal iron status. No studies have concluded that the introduction of WCM into the diet at 6 months of age produces adequate iron status in later infancy; however, recent studies have demonstrated that iron status is significantly impaired when WCM is introduced into the diet of 6-month-old infants. Data from studies abroad of highly iron-deficient infant populations suggest that infants fed partially modified milk formulas with supplemental iron in a highly bioavailable form (ferrous sulfate) may main- tam adequate iron status. However, these studies do not address the overall nutritional adequacy of the infant’s diet. Such formulas have not been studied in the United States. Optimal nutrition of the infant involves selecting the appropriate milk source and eventually introducing infant solid foods. To achieve this goal, the American Academy of Pediatrics recommends that infants be fed breast milk for the first 6 to 1 2 months. The Downloaded from by guest on October 1, 2016 ACADEMY AMERICAN OF PEDIATRICS 1107 microvillus. acceptable alternative to breast milk is ironfortified infant formula. Appropriate solid foods should be added between the ages of 4 and 6 months. Consumption of breast milk or iron-fortified formula, along with age-appropriate solid foods and juices, during the first 1 2 months of life allows for more balanced nutrition. The American Academy of Pediatrics recommends that whole cow’s milk and lowiron formulas not be used during the first year of life. only COMMFI-rEE ON 1991 NUTRITION, New 11. Bahna 12. Montalto 13. 14. 16. TO 17. MB, Benson milk feedings. AS, Martinez Martinez GA, 18. Ernst 19. Academy I Fomon Forbes AL, Adams Elwood PC. human subjects Iron and 4. American formulas. Andelman Academy of Pediatrics, Pediatrics. 23. 24. MB, Sered BR. Utilization Niccum WL, prevention 7. Marsh iron iron Jackson SW, Wright RL, Steams C. anemia H, Stierwalt fortification RP. The Use of ferric 26. WW, of age. Penrod E, Comparative of a milk formula for 27. Academy mentation 9, Fomon for infants, Si, Ziegler gastrointestinal ,0. cow’s Pediatr use of blood in the USE neonate, OF loss and iron ferrous Uptake, and WHOLE their sorting and infants. 33. relationship COW’S to the national prepared of in vitro, animal, Nutribioavail- studies preparations Reports Her Majesty’s of the absorption from bread. on Public Health Stationery by In: Panel and Office; on Medical 1968:1-30. in cereals. 1987;111:635-636 inhibition of inorganic iron 1983;84:90-101 FA. Consequences Oski I I Pediatr. RT. Calcium of starting whole cow milk at Pediatr. 1987;111:813-816 K, Acosta PB. Impact on iron status of life. J Pediatr 6 months of introducing Gastroenterol Nutr. M, Hutchinson of infants Haschke SW, Doucer months) fed H, Swartz WCM 5, Suskind fe-fortified + cereal. 1990;616:105A Nutr. EE, Rogers RR, et al. Iron absorption from infant 1989;26:250-254 Res. F, Pietschnig of infants (6-12 B, Vanura H, et al. Iron intake fed iron-fortified beikost with and iron nutritional Am J Clin meat. Nutr. Stekel A, Olivares milk Stekel Yip M, Pizzarro formulas A, Olivares M, Cayazzo fortification. R, Kinkin of fortification Nutr. iron 1986;43:917-922 M, et al. Prevention I Clin Am NJ, among F, et al. Absorption Am J Clin Nutr. in infants. of iron deficiency 1988;45:265-269 Fleshood L, Trowbridge low-income children FL. Declining the United in prevalence of States. JAMA. Yip R, Walsh KM. Goldfarb in childhood MG, Blinkin in a middle-class NJ. Declining prevalence setting: a pediatric formula should of success story? milk in iron 34. in to 35. Wilson or infant 1983;71 :984-985 cow’s milk, age, and be continued for Pediatrics. JF. Whole Ziegler EE, Fomon further observations Si, Nelson on Fomon SJ, Sanders 1990;1 16:690-696 36. Ziegler EE. Milk and 37. 579 Shank JS, Dorsey infants receiving in infancy: 1987;46:1 Pediatr. of Oski FA, behavior of macromolestructure Breast-feeding C. gastrointestinal bleeding. Pediat- SE, et al. Cow blood loss from milk the feeding in infancy: gastrointestinal tract. Pediatr. 1990;116:11-18 Iron supple- I Woodruff rics. 1984;73:879-880 1959;24:404- status. transport of 6- to 12- of four bioavailability: International Task Force report on iron Gastroenterology. Si, Ziegler 1 2 months. 38. WA. intake 1987;258:1619-1623 32. response feeding nutrition nutrient iron in commercially I: radioactive in the second Pediatr anemia 1976;58:765-768 milk infants 1985;139:1010- a summary MJ, et al. Comparison of iron Gastroenterol Fomon from 1953;86:553-567 on Nutrition. SE, et al. Cow of American AJDC. 1988;47:108-1 12 of by term Pediatrics. Committee Pediatrics. EE, Nelson 198198:540-545 Weaver LT, Walker cules 1108 of Pediatrics, and ME, Parmley GJ, DeWeir status 42 8. American the Pediatrics. 1987;80:330-334 hematologic infants. KA. Food of Health. JC, Anderson milk foods. Iron-fortified and AJDC. during I 17 in rats. 6 months / Iron balance role of fresh in infants. intakes formula. iron England: RM. Iron status 1972;124:26-30 of hypochromic A, Long Ministry number 25. Fuchs, 31. on Nutrition. of dietary States 1990;10:462-467 1971;45:55 1966;1 1:45-54 5, Woodruff CW, Wright iron deficiency. AJDC. in the United infancy. 1989;49:225-238 of various Tunnessen cow’s 1983;72:253-255 Committee of 1985;85:826-830 DJ. Nutrient of iron Group in flour, London, absorption AJDC. 6. Iron in Flour, Subjects. 30. Academy of Pediatrics, Committee on Nutrition, requirements in infancy. Pediatrics. 1969:43:34-42 milk during or infant CE, Arnaud Am I Clin Nutr. ability. 20. Publication The effect 1987;110:660-661 and clinical determinations tional Anemia Consultative 29. Nutrition. infants: low-fat of supplemental 28. on of older or cow milk: Pediatr. AAP Section 2. American 3. I cereals. JC, Conrad Committee of formula-fed 1986;5:331-341 FW. Feeding milk SJ. Bioavailability Barton Pediatrics. intakes 1985;75:343-351 1990;117:586-600 Pediatr. 22. Pediatrics, intakes fed formula SJ. Bioavailability in infancy. Nutrient MS. Richard Fomon of milk 1987;59:131-136 Nutrient Pediatrics. AS, Malec infants anemia cow’s Development. 1987;73:539-548 21. Section GA. I Am Coll Nutr. fed cow’s Brady JA, dry infant of Agriculture Liaison M. Lauer, MD, Ann Allergy. milk. GA, Krieger Ryan children surveys. REFERENCES whole JD. Gastrointestinal Martinez GA, Ryan AS. Nutrient intake first I 2 months of life. J Am Diet Assoc. by milk American fed cow’s different month-old Cardiology . infants Van S. 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Acosta milk or milk-based for older I infants. I Pediatr. 1990;1 PB. The vitamin formula, abstracted. P. of Pediatr. 17:576- E status of Fed Proc. 194 Honig AS, performance 1983;71:877-880 Downloaded from by guest on October 1, 2016 MILK Helu B, Howanitz in nonanemic, Effect iron-deficient iron infants. therapy Pediatrics. on 39. WaIter anemia Lozoff 40. R, De Andraca on infant B, Bittenham GM, iron therapy effects rics. 1987;79:981-995 41 42. . Pollitt E, Hathirat tional achievement Dobbing J. Brain, Springer-Verlag; I, Chadud psychomotor P. et al. Adverse Wolf on infant AW, developmental P. Kotchabhakdi in Thai Behavior 1990:195 effect of iron 43. deficiency Pediatr Res. 1988;23:650 et al. Iron deficiency anemia and development. children. test N, et al. Iron FASEB deficiency I. 1988;2:A1 and Iron in the Infant Pediat- performance. Diet. and educa- I 196. Abstract New 44. York, NY: Ben-Shachar D, Ashkenazi R, Youdim early iron-deficiency on dopaminergic Dev Neurosci. 1986;4:81-88 Yehuda S, Youdim reduced learning MH, MH. Long-term neurotransmission Mostofsky capacity in DI, rats. Brain consequence in rats. iron-deficiency Pharmacol of mt / causes Biochem Behav. 1986;25:141-144 45. Ben-Shachar blood-brain chem. D, Yehuda barrier and 5, Finberg insulin JPM, transport et al. Selective in iron-deficient alteration rats. / Neuro- 1988;50:1434-1437 Downloaded from by guest on October 1, 2016 ACADEMY AMERICAN OF PEDIATRICS 1109 in The Use of Whole Cow's Milk in Infancy Pediatrics 1992;89;1105 Updated Information & Services including high resolution figures, can be found at: /content/89/6/1105 Citations This article has been cited by 22 HighWire-hosted articles: /content/89/6/1105#related-urls Permissions & Licensing Information about reproducing this article in parts (figures, tables) or in its entirety can be found online at: /site/misc/Permissions.xhtml Reprints Information about ordering reprints can be found online: /site/misc/reprints.xhtml PEDIATRICS is the official journal of the American Academy of Pediatrics. A monthly publication, it has been published continuously since 1948. PEDIATRICS is owned, published, and trademarked by the American Academy of Pediatrics, 141 Northwest Point Boulevard, Elk Grove Village, Illinois, 60007. Copyright © 1992 by the American Academy of Pediatrics. All rights reserved. Print ISSN: 0031-4005. Online ISSN: 1098-4275. Downloaded from by guest on October 1, 2016 The Use of Whole Cow's Milk in Infancy Pediatrics 1992;89;1105 The online version of this article, along with updated information and services, is located on the World Wide Web at: /content/89/6/1105 PEDIATRICS is the official journal of the American Academy of Pediatrics. A monthly publication, it has been published continuously since 1948. PEDIATRICS is owned, published, and trademarked by the American Academy of Pediatrics, 141 Northwest Point Boulevard, Elk Grove Village, Illinois, 60007. Copyright © 1992 by the American Academy of Pediatrics. All rights reserved. Print ISSN: 0031-4005. Online ISSN: 1098-4275. Downloaded from by guest on October 1, 2016
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